Medical Affairs Consultant

17 hours, 3 minutes ago
Hire Digital

Hire Digital

Hire Digital connects businesses with top freelance talent in digital marketing, software development, and design, offering scalable solutions for digital growth and success.

Internet Software & Services
51-250
Founded 2015

Description

  • Lead the end-to-end review, update, and expansion of the RADIESSE® and ULTHERAPY® claims matrix.
  • Conduct structured literature reviews to identify new APAC-specific and broader regional clinical publications.
  • Critically appraise the quality, strength, and relevance of evidence supporting each product claim.
  • Determine which claims are defensible and distinguish between HCP-facing and consumer-facing substantiation.
  • Refine claim wording to ensure scientific accuracy, clarity, and appropriate caveats.
  • Establish a claim hierarchy and identify genuinely supported differentiating or competitive claims.
  • Validate references and maintain a complete reference library and source-documentation trail.
  • Identify evidence gaps and recommend priority claims and future evidence-generation opportunities.
  • Ensure recommendations align with medico-legal, regulatory, and internal review standards.
  • Present findings and recommendations to medical, marketing, and regulatory stakeholders.

Requirements

  • Hands-on experience in medical or scientific claims review, medico-legal review (MLR), regulatory affairs, or medical affairs within pharmaceuticals, medical devices, or aesthetics.
  • Strong critical-appraisal skills with confidence reviewing clinical literature, including study design, endpoints, statistics, and evidence grading.
  • Experience conducting literature reviews and validating references.
  • Solid understanding of promotional claim principles and how substantiation standards differ for HCP versus consumer communications.
  • Excellent scientific writing skills with strong accuracy and attention to detail.
  • Familiarity with aesthetics, dermatology, injectables, or energy-based devices (desirable).
  • Awareness of APAC regulatory nuances, local codes of practice, and regional evidence (desirable).

Interested in this position?

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